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President’s Message<br />

Laura Ziegler<br />

Greetings to the NARPA<br />

membership.<br />

Our next annual rights conference<br />

will take place in 2005, at a<br />

yet-to-be determined location in<br />

the Northeast. We look forward<br />

to seeing you there, and to maintaining<br />

the tradition of excellence<br />

that has marked NARPA<br />

conferences since 1981.<br />

What about 2004?<br />

NARPA is undergoing a transition<br />

aimed at strengthening the<br />

organization and enabling it to continue its mission in a<br />

changing political and economic landscape. We hope to<br />

expand member participation in NARPA’s work, to find<br />

additional funding sources, and especially, to make our<br />

conferences more financially sustainable — both for<br />

NARPA and for attendees. Among other things, we are<br />

exploring alternatives to the upscale hotels where we’ve<br />

met for the past 22 years, and more effective collaborations<br />

with other advocacy organizations.<br />

State governments, advocacy agencies, foundations and<br />

activist groups have something in common: fewer resources<br />

than before. Funding for attending out-of-state<br />

conferences has diminished. We will do our best to adapt,<br />

because it is critical that our work continue.<br />

These are perilous times. The foundations of our judicial<br />

system are shaking, fissures have opened in the bedrock<br />

of liberty and the rule of law can no longer be presumed.<br />

People without disability labels are now targeted<br />

for extended detention with no criminal charges, while<br />

all of us are advised to watch what we say — and, perhaps,<br />

what we think. The federal government announces<br />

“New Freedom” for people with disabilities to live independent<br />

lives outside of institutions, while waging a war<br />

of attrition on the human services, housing subsidies and<br />

entitlement programs which could make that freedom<br />

possible. Meanwhile we face expanded mandates for outpatient<br />

commitment, the pathologizing and drugging of<br />

almost every aspect of life, aggressive marketing disguised<br />

as science, and hate campaigns under the banner of advocacy.<br />

Coercion and force are promoted as enablers,<br />

couched in rhetoric that substitutes “voluntary submission”<br />

for self determination and clinical discretion for<br />

due process.<br />

Yet the ground shifts in more ways than one. The vision<br />

of recovery is gaining official endorsement, and reactionary<br />

attacks on peer run service models and cultural<br />

competency can be viewed as a kind of testament<br />

to their growing acceptance. Restraints-as-usual has been<br />

rejected by a significant part of the mental health establishment.<br />

The pharmaceutical industry’s gross overreaching<br />

and ethical shortfalls have brought it under critical<br />

scrutiny that is increasingly mainstream. Recognition of<br />

President’s Message continued on page 13<br />

NARPA Rights Tenet: Summer 2004 page 4<br />

NARPA/NAPAS<br />

Dialogue<br />

Bill Stewart<br />

The latest round of discussions<br />

between NARPA and the<br />

National Association of Protection<br />

and Advocacy Systems<br />

(NAPAS) was held during our<br />

annual conference in Austin on<br />

November 23, 2003. Our goals<br />

including pursuing a set of agreements<br />

for coordination of activities<br />

between the two groups. Ultimately,<br />

this discussion needs to<br />

culminate in a broader model of<br />

collaboration between groups with similar goals, but different<br />

strategies and circumstance. This is a summary of<br />

the status of those agreements:<br />

1.Several persons said that NARPA should play a role<br />

in development of individual advocacy groups of consumer/survivors.<br />

Many P&As depend on input from consumer/survivors<br />

to develop systems priorities, but in many<br />

states, the movement is co-opted by service providers or<br />

by NAMI or both. There were multiple requests from<br />

P&As for help in getting consumer/survivors to apply<br />

for PAIMI Advisory Councils. (STATUS: NARPA is pursuing<br />

a set of possible funding sources, keeping in mind<br />

our philosophy that accepting funds from government or<br />

for-profit sources is likely to compromise our autonomy.)<br />

2.There was strong agreement that NAPAS and NARPA<br />

should have better electronic information sharing.<br />

Maureen Fitzgerald (NAPAS president) said that Elizabeth<br />

Priaux of NAPAS has volunteered to act as liaison<br />

for NAPAS in the ongoing interaction between the two<br />

organizations. Both organizations agree that sharing and<br />

distributing specific information is advantageous.<br />

3.There was general agreement that NARPA should<br />

consider becoming an associate member of NAPAS, with<br />

two persons suggesting that the fee for associate membership<br />

be waived in light of NARPA’S financial circumstances.<br />

4.At least two participants expressed concern that their<br />

respective P&As were unresponsive and “arrogant” in<br />

their choices of issues taken as priorities for litigation.<br />

Discussion followed of the priority-setting process and<br />

the role of NAPAS when complaints about P&As are<br />

made. Maureen Fitzgerald said that NAPAS is a trade<br />

organization and that the federal agency responsible for<br />

oversight of P&As is in process of creating teams to visit<br />

respective states. (STATUS: Problems with individual<br />

Protection and Advocacy programs are a long-standing<br />

source of contentiousness between our respective groups.<br />

We continue to look for ways to have some productive<br />

outcomes as a result of this dialogue.)<br />

5.We had a discussion of trans-disability issues. A previous<br />

evening workshop revealed some of the differences<br />

NARPA/NAPAS Dialogue continued on page 19

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